chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98891846288918463TC8GENIChomozygous117852672
98891847188918472CA12GENIChomozygous117888004
98891851288918513GA15GENIChomozygous117852673
98891852888918529TC18GENIChomozygous117852674
98891872288918723GC14GENIChomozygous117852675
98891910388919104GA10GENIChomozygous117852676
98891911688919117GA7GENIChomozygous117852677
98891912788919128CT6GENIChomozygous117852678
98891916588919166AT10GENIChomozygous117852681
98891918488919185CA15GENIChomozygous117888024
98891929988919300CT13GENIChomozygous117888026
98891944788919448GT19GENIChomozygous117852683
98891957888919579CA15GENIChomozygous117852684
98891968088919681CT20GENIChomozygous117888032
98891977288919773AG12GENIChomozygous117888034
98891978988919790CT14GENIChomozygous117888036
98891990388919904TA14GENIChomozygous117852685
98891995288919953TC16GENIChomozygous117852686
98891997488919975CT13GENIChomozygous117852687
98892000888920009TC4GENIChomozygous117852688
98892024088920241TG10GENIChomozygous117852689
98892038588920386GC19GENIChomozygous117888048
98892051788920518CT19GENIChomozygous117888050
98892071188920712AG14GENIChomozygous117852691